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Immobilization of Gold Nanoparticles on Postsynthetically Modified NU-1000 for Hydrogen Evolution Reaction.
Muhamed, Shamna; Aparna, Ravari Kandy; Karmakar, Arun; Kundu, Subrata; Mandal, Sukhendu.
  • Muhamed S; School of Chemistry, Indian Institute of Science Education and Research Thiruvananthapuram, Thiruvananthapuram, Kerala 695551, India.
  • Aparna RK; School of Chemistry, Indian Institute of Science Education and Research Thiruvananthapuram, Thiruvananthapuram, Kerala 695551, India.
  • Karmakar A; Electrochemical Process Engineering (EPE) Division, CSIR-Central Electrochemical Research Institute (CECRI), Karaikudi, Tamil Nadu 630006, India.
  • Kundu S; Electrochemical Process Engineering (EPE) Division, CSIR-Central Electrochemical Research Institute (CECRI), Karaikudi, Tamil Nadu 630006, India.
  • Mandal S; School of Chemistry, Indian Institute of Science Education and Research Thiruvananthapuram, Thiruvananthapuram, Kerala 695551, India.
Inorg Chem ; 62(19): 7195-7202, 2023 May 15.
Article en En | MEDLINE | ID: mdl-37132510
ABSTRACT
NU-1000, being a hydrothermally stable metal-organic framework (MOF), with structural robustness is viable for functionalization with various entities. A postsynthetic modification strategy called solvent-assisted ligand incorporation (SALI) is chosen for functionalizing NU-1000 with thiol moieties using 2-mercaptobenzoic acid. In accordance with soft acid-soft base interactions, the thiol groups on NU-1000, as a scaffold, can immobilize the gold nanoparticles without much aggregation. The catalytically active gold sites on thiolated NU-1000 are utilized for hydrogen evolution reaction (HER). The catalyst delivered an overpotential of 101 mV at a current density of 10 mAcm-2 in 0.5 M H2SO4. The faster charge transfer kinetics determined from the Tafel slope of 44 mV/dec enhances the HER activity. The sustainable performance of the catalyst for 36 h proves its utility as a potential catalyst to produce neat hydrogen.

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2023 Tipo del documento: Article